Comparative proteomic analysis of early salt stress-responsive proteins in roots of SnRK2 transgenic rice

被引:78
作者
Nam, Myung Hee [2 ]
Huh, Sun Mi [1 ]
Kim, Kyung Mi [2 ]
Park, Woong June [3 ,4 ]
Seo, Jong Bok [2 ]
Cho, Kun [5 ]
Kim, Dool Yi [1 ]
Kim, Beom Gi [1 ]
Yoon, In Sun [1 ]
机构
[1] Natl Acad Agr Sci, Biocrops Dev Div, Suwon 441857, South Korea
[2] Korea Basic Sci Inst, Seoul Ctr, Seoul 136701, South Korea
[3] Dankook Univ, Dept Mol Biol, Yongin 448701, Gyeonggi Do, South Korea
[4] Dankook Univ, Inst Nanosensor & Biotechnol, Yongin 448701, Gyeonggi Do, South Korea
[5] Korea Basic Sci Inst, Div Mass Spectrometry, Ochang 363883, South Korea
关键词
ORYZA-SATIVA L; ABSCISIC-ACID; DIFFERENTIAL EXPRESSION; HYPEROSMOTIC STRESS; SIGNAL-TRANSDUCTION; TRANSCRIPT LEVELS; HIGHER-PLANT; KINASE; TOLERANCE; IDENTIFICATION;
D O I
10.1186/1477-5956-10-25
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background: The rice roots are highly salt-sensitive organ and primary root growth is rapidly suppressed by salt stress. Sucrose nonfermenting 1-related protein kinase2 (SnRK2) family is one of the key regulator of hyper-osmotic stress signalling in various plant cells. To understand early salt response of rice roots and identify SnRK2 signaling components, proteome changes of transgenic rice roots over-expressing OSRK1, a rice SnRK2 kinase were investigated. Results: Proteomes were analyzed by two-dimensional electrophoresis and protein spots were identified by LC-MS/MS from wild type and OSRK1 transgenic rice roots exposed to 150 mM NaCl for either 3 h or 7 h. Fifty two early salt -responsive protein spots were identified from wild type rice roots. The major up-regulated proteins were enzymes related to energy regulation, amino acid metabolism, methylglyoxal detoxification, redox regulation and protein turnover. It is noted that enzymes known to be involved in GA-induced root growth such as fructose bisphosphate aldolase and methylmalonate semialdehyde dehydrogenase were clearly down-regulated. In contrast to wild type rice roots, only a few proteins were changed by salt stress in OSRK1 transgenic rice roots. A comparative quantitative analysis of the proteome level indicated that forty three early salt-responsive proteins were magnified in transgenic rice roots at unstressed condition. These proteins contain single or multiple potential SnRK2 recognition motives. In vitro kinase assay revealed that one of the identified proteome, calreticulin is a good substrate of OSRK1. Conclusions: Our present data implicate that rice roots rapidly changed broad spectrum of energy metabolism upon challenging salt stress, and suppression of GA signaling by salt stress may be responsible for the rapid arrest of root growth and development. The broad spectrum of functional categories of proteins affected by over-expression of OSRK1 indicates that OSRK1 is an upstream regulator of stress signaling in rice roots. Enzymes involved in glycolysis, branched amino acid catabolism, dnaK-type molecular chaperone, calcium binding protein, Sal T and glyoxalase are potential targets of OSRK1 in rice roots under salt stress that need to be further investigated.
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页数:19
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共 99 条
[1]   Proteome Analysis of Potato under Salt Stress [J].
Aghaei, Keyvan ;
Ehsanpour, Ali Akbar ;
Komatsu, Setsuko .
JOURNAL OF PROTEOME RESEARCH, 2008, 7 (11) :4858-4868
[2]   Potato Responds to Salt Stress by Increased Activity of Antioxidant Enzymes [J].
Aghaei, Keyvan ;
Ehsanpour, Ali Akber ;
Komatsu, Setsuko .
JOURNAL OF INTEGRATIVE PLANT BIOLOGY, 2009, 51 (12) :1095-1103
[3]   ABA-Dependent and -Independent G-Protein Signaling in Arabidopsis Roots Revealed through an iTRAQ Proteomics Approach [J].
Alvarez, Sophie ;
Hicks, Leslie M. ;
Pandey, Sona .
JOURNAL OF PROTEOME RESEARCH, 2011, 10 (07) :3107-3122
[4]   Functional characterisation of OsCPK21, a calcium-dependent protein kinase that confers salt tolerance in rice [J].
Asano, Takayuki ;
Hakata, Makoto ;
Nakamura, Hidemitsu ;
Aoki, Naohiro ;
Komatsu, Setsuko ;
Ichikawa, Hiroaki ;
Hirochika, Hirohiko ;
Ohsugi, Ryu .
PLANT MOLECULAR BIOLOGY, 2011, 75 (1-2) :179-191
[5]   Plant calreticulin is specifically and efficiently phosphorylated by protein kinase CK2 [J].
Baldan, B ;
Navazio, L ;
Friso, A ;
Mariani, P ;
Meggio, F .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1996, 221 (03) :498-502
[6]   Targeting detoxification pathways: an efficient approach to obtain plants with multiple stress tolerance? [J].
Bartels, D .
TRENDS IN PLANT SCIENCE, 2001, 6 (07) :284-286
[7]   Identification of nine sucrose nonfermenting 1-related protein kinases 2 activated by hyperosmotic and saline stresses in Arabidopsis thaliana [J].
Boudsocq, M ;
Barbier-Brygoo, H ;
Laurière, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (40) :41758-41766
[8]   A rice dehydration-inducible SNF1-related protein kinase 2 phosphorylates an abscisic acid responsive element-binding factor and associates with ABA signaling [J].
Chae, Min-Ju ;
Lee, Jung-Sook ;
Nam, Myung-Hee ;
Cho, Kun ;
Hong, Ji-Yeon ;
Yi, Sang-A ;
Suh, Seok-Cheol ;
Yoon, In-Sun .
PLANT MOLECULAR BIOLOGY, 2007, 63 (02) :151-169
[9]   Salt-induced protein synthesis in tomato roots: the role of ABA [J].
Chen, CCS ;
Plant, AL .
JOURNAL OF EXPERIMENTAL BOTANY, 1999, 50 (334) :677-687
[10]   New changes in the plasma-membrane-associated proteome of rice roots under salt stress [J].
Cheng, Yanwei ;
Qi, Yaocheng ;
Zhu, Qian ;
Chen, Xi ;
Wang, Ning ;
Zhao, Xin ;
Chen, Haiyan ;
Cui, Xiangju ;
Xu, Langlai ;
Zhang, Wei .
PROTEOMICS, 2009, 9 (11) :3100-3114